Radiation Free Study

Not Applicable

Not yet recruiting

• Conditions: Aortic Aneurysm

• Registration Number: NCT06549348
• Lead Sponsor: Philips Clinical & Medical Affairs Global

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-8-8
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Not yet recruiting
• Sex: All
• Target Recruitment: 182

Inclusion Criteria

Inclusion Criteria:<br><br> - Subject will be undergoing a primary Fenestrated Endovascular Aortic Repair (FEVAR)<br> procedure (including subjects with prior infrarenal EVAR or open repair) that<br> includes the incorporation of visceral arteries into the repair.<br><br> - Subject is able to give informed consent and is 18 years of age or older, or of<br> legal age to give informed consent per state or national law.<br><br> - Subject has a life expectancy of at least 2 years<br><br> - Target vessels to be included are the Celiac Trunk, Superior Mesenteric Artery and<br> Renal Arteries<br><br>Exclusion Criteria:<br><br> - Subjects undergoing an endovascular procedure that include branches or iliac<br> branched devices (IBD) in the repair<br><br> - Subject treated for re-intervention / staged procedure post-primary FEVAR procedure<br><br> - Subjects intended to be treated for more than 4 target vessels (not counting the<br> contralateral gate)<br><br> - Subject treated for an emergent (<24hrs after emergence) procedure<br><br> - Subject with connective tissue disorder eg, Marfan's or Ehlers Danlos Syndrome<br><br> - Subject with contrast allergies<br><br> - Subject participates in a potentially confounding drug or device trial during the<br> course of the study. Co-enrollment in concurrent trials may be allowed provided that<br> pre-approval is obtained from Philips.<br><br> - All vulnerable subjects such as immuno-compromised subjects, subjects lacking the<br> capacity to provide consent, patients in emergency situations, pregnant or<br> breast-feeding women, or any other subject who meets an exclusion criteria,<br> according to applicable national laws, if any.<br><br> - Subject unwilling or unable to comply with the protocol unable to understand verbal<br> and/or written informed consent

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To demonstrate that the average procedure fluoroscopy time using LumiGuide is lower compared to conventional fluoroscopy guidance in Fenestrated Endovascular Aortic Repair (FEVAR).